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1.
Int J Cardiol Heart Vasc ; 50: 101336, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38304727

ABSTRACT

Background: Anti-cancer treatment can be fraught with cardiovascular complications, which is the most common cause of death among oncological survivors. Without appropriate cardiomonitoring during anti-cancer treatment, it becomes challenging to detect early signs of cardiovascular complications. In order to achieve higher survival rates, it is necessary to monitor oncological patients outpatiently after anti-cancer treatment administration. In this regard, we aim to evaluate the efficacy of single-lead ECG remote monitoring to detect cardiotoxicity in cancer patients with minimal cardiovascular diseases after the first cycle of polychemotherapy. Materials and methods: The study included patients 162 patients over 18 years old with first diagnosed different types of solid tumors, planed for adjuvant (within 8 weeks after surgery) or neoadjuvant polychemotherapy. All patients were monitored, outpatiently, during 14-21 days (depending on the regimen of polychemotherapy) after polychemotherapy administration using single-lead ECG. Results: QTc > 500 mc prolongation was detected in 8 patients (6.6 %), first-diagnosed arial fibrillation was detected in 11 patients (9 %) in period after chemotherapy administration. Moreover, left ventricular diastolic dysfunction using single-lead ECG after polychemotherapy was detected in 49 (40.1 %) patients with sensitivity 80 %, specificity 95 %, AUC 0.88 (95 % CI, 0.82-0.93). Conclusions: The side effects of cancer treatment may cause life-threatening risks. Early identification of cardiotoxicity plays a vital role in the solution of this problem. Using portable devices to detect early cardiotoxicity is a simple, convenient and affordable screening method, that can be used for promptly observation of patients.

2.
Article in English | MEDLINE | ID: mdl-30039765

ABSTRACT

Atherothrombosis-related diseases are one of the world's leading causes of mortality, and thus the search for new therapeutic approaches in this area remains a very urgent task. Modern pharmacogenomic technologies make it possible to obtain valuable data on disease pathogenesis and optimal therapeutic approaches. One promising research direction is the study of the thromboxane A2 - thromboxane A synthase - thromboxane A2 receptor axis. This review summarizes the recent evidence and suggests that systematic works in this area are creating new and promising opportunities in the treatment of patients with cardiovascular diseases.


Subject(s)
Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/metabolism , Enzyme Inhibitors/therapeutic use , Molecular Targeted Therapy , Thromboxane-A Synthase/antagonists & inhibitors , Thromboxane-A Synthase/metabolism , Animals , Cardiovascular Diseases/genetics , Cardiovascular Diseases/pathology , Drug Discovery/methods , Enzyme Inhibitors/pharmacology , Humans , Molecular Targeted Therapy/methods , Pharmacogenomic Testing , Platelet Aggregation/drug effects , Polymorphism, Genetic , Receptors, Thromboxane A2, Prostaglandin H2/metabolism , Signal Transduction/drug effects , Thromboxane A2/metabolism , Thromboxane-A Synthase/genetics
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